@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_head
{
this:
np:hasAssertion
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion
;
np:hasProvenance
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance
;
np:hasPublicationInfo
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion
a
np:Assertion
.
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance
a
np:Provenance
.
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion
{
miriam-gene:6683
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGN75adfc48ba9e0969954847e8e14219aa
sio:SIO_000628
miriam-gene:6683
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_provenance
{
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_assertion
dcterms:description
"[Other features noted in this kindred including epilepsy, cognitive impairment, depression, and migraine did not segregate with the HSP phenotype or mutation, and therefore the significance of these features to SPG4 is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15667412
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP868861.RAFpLehrb0PuhX7Vjm0SJivwTZBtSY5eTeR_VL5n6f3NY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}